rs397507902

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;T)	6	BRCA2 variant considered pathogenic for breast cancer
(T;T)	0	common in clinvar

Make rs397507902(A;A)

Make rs397507902(A;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32319080

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507902
dbSNP (classic)	rs397507902
ClinGen	rs397507902
ebi	rs397507902
HLI	rs397507902
Exac	rs397507902
Gnomad	rs397507902
Varsome	rs397507902
LitVar	rs397507902
Map	rs397507902
PheGenI	rs397507902
Biobank	rs397507902
1000 genomes	rs397507902
hgdp	rs397507902
ensembl	rs397507902
geneview	rs397507902
scholar	rs397507902
google	rs397507902
pharmgkb	rs397507902
gwascentral	rs397507902
openSNP	rs397507902
23andMe	rs397507902
SNPshot	rs397507902
SNPdbe	rs397507902
MSV3d	rs397507902
GWAS Ctlg	rs397507902

Max Magnitude

6

ClinVar
Risk	rs397507902(A;A) rs397507902(G;G)
Alt	rs397507902(A;A) rs397507902(G;G)
Reference	Rs397507902(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32893217T>A; NC_000013.10:g.32893217T>G
CLNSRC	ClinVar
CLNACC	RCV000045162.2, RCV000257036.2,